Affiliation:
1. Postgraduate Course of Tropical Medicine and Infectology, Laboratory of Immunology, Federal University of Triângulo Mineiro, Avenida Getúlio Guaritá S/N, 38015-050 Uberaba, MG, Brazil
2. Postgraduate Course of Tropical Medicine and Infectology, Laboratory of Parasitology, Federal University of Triângulo Mineiro, Uberaba, MG, Brazil
Abstract
Dendritic cells (DCs) are major immune components, and depending on how these cells are modulated, the protective host immune response changes drastically.Trypanosoma cruziis a parasite with high genetic variability and modulates DCs by interfering with their capacity for antigen recognition, migration, and maturation. Despite recent efforts, the association between DCs andT. cruziI (TcI) and TcII populations is unknown. Herein, it was demonstrated that AQ1.7 and MUTUM TcI strains present low rates of invasion of bone marrow-derived DCs, whereas the 1849 and 2369 TcII strains present higher rates. Whereas the four strains similarly induced the expression of PD-L1, the production and expression of IL-10 and TLR-2, respectively, in DCs were differentially increased. The production of TNF-α, IL-12, IL-6, and CCL2 and the expression of CD40, CD80, MHC-II, CCR5, and CCR7 changed depending on the strain. The 2369 strain yielded the most remarkable results because greater invasion correlated with an increase in the levels of anti-inflammatory molecules IL-10 and PD-L1 but not with a change in the levels of TNF-α, MHC-II, or CD40 molecules. These results suggest thatT. cruzistrains belonging to different populations have evolved specific evasion strategies that subvert DCs and consequently the host response.
Funder
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Subject
Immunology,General Medicine,Immunology and Allergy
Cited by
28 articles.
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